Clinical Research Nurse Coordinator
Apply NowCompany: ERA Health Research
Location: Redmond, WA 98052
Description:
ERA Health Research is a fast-growing clinical research company that is seeking a Clinical Research Nurse Coordinator who will play a critical role in supporting clinical research activities within the clinical site.
The Clinical Research Nurse Coordinator role requires hands-on patient care, meticulous attention to compliance standards, and collaboration with multidisciplinary teams to ensure the success of clinical trials conducted at the site.
ESSENTIAL DUTIES
EDUCATION & EXPERIENCE
REQUIRED
PREFERRED
OTHER DUTIES
In addition to the specific responsibilities outlined above, this role may perform other tasks or projects as assigned by a supervisor or manager. These additional duties will fall within the scope of the role and contribute to the overall success of the team.
COMPENSATION
$45.00-$50.00/hourly
EEO STATEMENT
Eastside Research Associates provides equal employment opportunities to all without regard to race, color, religion, sex (including sexual orientation or gender identity), national origin, age, disability, genetic information, or other protected status. Applicants and employees with disabilities may be entitled to reasonable accommodations under the terms of the Americans with Disabilities Act and certain state or local laws. A reasonable accommodation is an adjustment to our standard application and/or interview and/or employment process which will ensure an equal employment opportunity without imposing undue hardship on Eastside Research Associates. Please inform our team if you are requesting accommodation to complete any forms or otherwise participate in the application process or perform the essential functions of this role.
The Clinical Research Nurse Coordinator role requires hands-on patient care, meticulous attention to compliance standards, and collaboration with multidisciplinary teams to ensure the success of clinical trials conducted at the site.
ESSENTIAL DUTIES
- Clinical Trial Coordination: Oversee and coordinate the day-to-day operations of clinical trials conducted at the site, ensuring adherence to protocols, timelines, and site-specific requirements.
- Eligibility Assessment: Review patients' medical records to assess eligibility for clinical studies, ensuring alignment with inclusion/exclusion criteria.
- Patient Consent: Obtain informed consent from patients participating in clinical research studies, adhering to ethical and regulatory standards.
- Documentation Management: Maintain accurate and organized case report forms, charts, and essential records to ensure compliance and data integrity.
- Clinical Procedures: Perform clinical tasks integral to research protocols, including monitoring vital signs, conducting venipuncture/phlebotomy, performing nasal swabs, and dispensing and tracking study medications.
- Compliance Monitoring: Guarantee strict compliance with research protocols, Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), and all applicable laws, regulations, and clinical site policies.
- Liaison Role: Serve as a point of contact between clinical teams, patients, sponsors, and investigators, ensuring seamless communication and coordination.
- Regulatory Support: Prepare, submit, and manage Institutional Review Board (IRB) correspondence and regulatory documentation, ensuring adherence to clinical site requirements.
- Quality Assurance: Consistently follow site-specific standards, GCP guidelines, and applicable regulatory requirements to maintain the highest level of research integrity.
EDUCATION & EXPERIENCE
REQUIRED
- Bachelor's degree in nursing or a related field.
- Current Registered Nurse (RN) license in the applicable state.
- Proficiency in performing clinical procedures, including phlebotomy, vital signs monitoring, and medication handling.
- Familiarity with Institutional Review Board (IRB) requirements and regulatory processes.
- Excellent organizational and time management skills to handle multiple tasks effectively.
- Attention to detail for accurate documentation and compliance monitoring.
- Strong interpersonal skills for patient interaction and team collaboration.
- Strong problem-solving and critical-thinking abilities.
PREFERRED
- Minimum of 1-2 years of experience in clinical research or nursing.
- Knowledge of clinical research protocols, Good Clinical Practice (GCP), and regulatory guidelines.
- Certification in clinical research (e.g., CCRC).
- Basic proficiency in clinical data management systems and electronic health records.
OTHER DUTIES
In addition to the specific responsibilities outlined above, this role may perform other tasks or projects as assigned by a supervisor or manager. These additional duties will fall within the scope of the role and contribute to the overall success of the team.
COMPENSATION
$45.00-$50.00/hourly
EEO STATEMENT
Eastside Research Associates provides equal employment opportunities to all without regard to race, color, religion, sex (including sexual orientation or gender identity), national origin, age, disability, genetic information, or other protected status. Applicants and employees with disabilities may be entitled to reasonable accommodations under the terms of the Americans with Disabilities Act and certain state or local laws. A reasonable accommodation is an adjustment to our standard application and/or interview and/or employment process which will ensure an equal employment opportunity without imposing undue hardship on Eastside Research Associates. Please inform our team if you are requesting accommodation to complete any forms or otherwise participate in the application process or perform the essential functions of this role.